Automatic disinfecting and drying equipment and method for medical orthopedic instruments

Abstract

The invention relates to the technical field of intelligent disinfection, and particularly discloses an automatic disinfection and drying device and method for medical orthopedic instruments, and the device comprises an instrument processing module which is used for carrying out the preliminary judgment of a target medical orthopedic instrument, and obtaining the real-time instrument data; the intelligent disinfection module is used for determining an intelligent disinfection scheme by combining the instrument material and the disinfection demand with the real-time instrument data, and performing intelligent disinfection based on the intelligent disinfection scheme to obtain first instrument data; the drying processing module is used for screening a drying mode with the highest matching degree based on the first instrument data to perform instrument drying, so that second instrument data is obtained; the equipment inspection module is used for performing data inspection on the second instrument data so as to judge whether the target medical orthopedic instrument can meet the real-time use requirement or not based on a data inspection result, and if yes, it is judged that disinfection and drying are qualified; the automatic disinfecting and drying capacity of the medical orthopedic instrument is improved, and the medical orthopedic instrument is disinfected and dried more accurately and efficiently.

Description

Technical Field

[0001] This invention relates to the field of intelligent disinfection technology, and in particular to an automatic disinfection and drying device and method for medical orthopedic instruments. Background Technology

[0002] Currently, in the medical field, especially in orthopedic medicine, the sterilization of medical devices plays a crucial role, directly impacting patient safety. To ensure these devices meet sterility standards in clinical use and avoid infection risks for patients, all medical devices planned for reuse within hospitals must undergo rigorous sterilization and drying procedures.

[0003] However, traditional sterilization and drying methods typically rely on manual operation, which is not only inefficient but also makes it difficult to ensure comprehensive and thorough sterilization. This is especially true for orthopedic instruments with folded parts, such as scissors and forceps, where manual sterilization often fails to reach all areas, leaving bacterial residues and posing safety hazards.

[0004] Therefore, this invention proposes an automatic disinfection and drying device and method for medical orthopedic instruments. Summary of the Invention

[0005] This invention provides an automated disinfection and drying device and method for medical orthopedic instruments. It involves preliminary assessment of the target medical orthopedic instrument to obtain real-time instrument data, and determining an intelligent disinfection scheme suitable for the target medical orthopedic instrument based on its material and disinfection requirements. Intelligent disinfection is then performed, followed by drying using a non-destructive drying mode. The dried target medical orthopedic instrument is then inspected, thereby improving the efficiency and accuracy of disinfection and drying while maximizing the safe use of the instrument.

[0006] This invention provides an automatic sterilization and drying device for medical orthopedic instruments, comprising: The instrument processing module is used to make a preliminary judgment on the target orthopedic medical instrument based on preset sensors, and to obtain real-time instrument data of the target orthopedic medical instrument in the preliminary judgment. The intelligent disinfection module is used to determine an intelligent disinfection plan for the target orthopedic medical device by combining the device material and the disinfection requirements of the target orthopedic medical device with real-time device data, and to perform intelligent disinfection of the target orthopedic medical device based on the intelligent disinfection plan, thereby obtaining the first device data after disinfection. The drying module is used to dry the target orthopedic medical device by selecting the drying mode with the highest matching degree based on the first device data, thereby obtaining the second device data after drying. The equipment inspection module is used to inspect the data of the second instrument, and then determine whether the target medical orthopedic instrument can meet the real-time use requirements based on the data inspection results. If it does, the disinfection and drying of the target medical orthopedic instrument is deemed qualified.

[0007] Preferably, the instrument processing module includes: Preliminary identification unit: used to perform preliminary identification of target orthopedic medical devices based on preset sensors to obtain initial device data; Type determination unit: used to classify the target orthopedic medical device by type based on the initial device data, and obtain the first set of device types of the target orthopedic medical device; Comprehensive Judgment Unit: Used to combine the first set of instrument types with the initial instrument data to determine whether the target medical orthopedic instrument needs to be disinfected and dried; If the target orthopedic medical device needs to be sterilized and dried, the initial device data will be standardized to obtain the real-time device data of the target orthopedic medical device. Conversely, there is no need to sterilize and dry the target orthopedic medical device.

[0008] Preferably, the intelligent disinfection module includes: Solution screening unit: used to identify the material of the target medical orthopedic device based on preset sensors, and determine the disinfection treatment plan for each target medical orthopedic device based on the preset material database, so as to obtain an initial disinfection treatment plan table; Disinfection treatment unit: used to extract the disinfection treatment plan that meets the requirements of each target medical orthopedic device based on the initial disinfection treatment plan table, and use it as the initial disinfection treatment plan; Disinfection optimization unit: used to determine the number of target orthopedic medical instruments based on real-time instrument data, and optimize the initial disinfection treatment plan based on the number of instruments to obtain an optimized disinfection plan; The second optimization unit is used to obtain the real-time usage requirements of the target medical orthopedic device to determine the corresponding disinfection requirements, and to optimize the disinfection optimization scheme based on the disinfection requirements to obtain the second optimization scheme. Disinfection scheme unit: used to input the second optimized scheme and real-time instrument data into the preset disinfection treatment model, thereby determining the intelligent disinfection scheme for the target medical orthopedic instrument; Parameter adjustment unit: used to acquire the real-time equipment parameters of the target disinfection and drying equipment, and to determine the parameter adjustment strategy for the target disinfection and drying equipment based on the intelligent disinfection scheme and the real-time equipment parameters. Strategy execution unit: used to adjust the strategy based on parameters and transmit it to the target disinfection and drying equipment for intelligent disinfection; Status detection unit: used to acquire the equipment status parameters at each detection moment of the current intelligent disinfection cycle when intelligently disinfecting the target disinfection and drying equipment, and obtain the equipment status parameter set; Parameter classification unit: used to classify the set of device status parameters based on different device types to obtain the first category parameter set; Performance Analysis Unit: Used to sort the equipment status parameters of each subset of the first category parameter set based on time series, thereby comprehensively judging the equipment stability performance of the target disinfection and drying equipment based on the sorting results, and optimizing the intelligent disinfection scheme in a timely manner based on the equipment stability performance; Data extraction unit: Used to collect real-time instrument data of the target medical orthopedic instrument after intelligent disinfection, and to process the data to obtain the first instrument data.

[0009] Preferably, the performance analysis unit includes: First sorting subunit: used to sort the device status parameters of each first category parameter subset in the first category parameter set based on the time series, to obtain the first ordered parameter set; Curve fitting subunit: Used to input the device state parameters in each first ordered parameter subset of the first ordered parameter set into the same coordinate system and perform curve fitting to obtain the first state parameter curve corresponding to each first ordered parameter subset; Performance Judgment Subunit: Used to judge the parameter performance of the equipment state parameter corresponding to each first state parameter curve based on the degree of curve fluctuation of the first state parameter curve, so as to comprehensively determine the equipment stability performance of the target disinfection and drying equipment.

[0010] Preferably, the performance judgment subunit includes: The parameter performance Z of the device state parameter corresponding to each first state parameter curve is determined based on the degree of curve fluctuation of the first state parameter curve. Where Z represents the parametric performance of the current first state parameter curve. The exponential weight of the stability index of the current first state parameter curve. The exponential weight of the fluctuation exponent of the current first state parameter curve. The exponential weight of the outlier index of the current first state parameter curve is given by N, where N is the number of state parameter points in the current first state parameter curve. This represents the difference between the parameter value corresponding to the state parameter point in the current first state parameter curve and the corresponding value on the first state parameter curve. This represents the state parameter value corresponding to the i-th state parameter point in the current first state parameter curve. Let be the curve parameter value corresponding to the i-th state parameter point in the current first state parameter curve, and b be the maximum parameter difference corresponding to the current first state parameter curve. Let be the standard deviation of the curve parameter value corresponding to each state parameter point in the first state parameter curve, m be the average value of the curve parameter value corresponding to each state parameter point in the first state parameter curve, and e be the logarithm of the natural base.

[0011] Preferably, the drying module includes: Drying comparison unit: used to compare the first instrument data with each drying mode in the drying database, thereby extracting the drying mode with the highest matching degree with the first instrument data as the first drying mode; Drying strategy unit: used to determine the equipment parameter adjustment strategy for the target disinfection and drying equipment based on the first drying mode; Drying execution unit: used to dry the target medical orthopedic device based on the equipment parameter adjustment strategy, and to obtain the real-time device data after drying based on the preset sensors to obtain the second device data of the target medical orthopedic device.

[0012] Preferably, the equipment inspection module includes: Data verification unit: used to verify the second device data based on the disinfection and drying requirements of the target medical orthopedic device, thereby obtaining the first verification data; The comparison unit is used to compare the first test data with the standard disinfection and drying data range. If each initial test data falls within the standard sterilization and drying data range, the initial test of the target medical orthopedic device is deemed qualified. If any of the first test data is not within the range of standard disinfection and drying data, the target medical orthopedic device needs to be disinfected and dried again. Functional testing unit: used to determine the functional integrity of the target orthopedic medical device based on the initial qualified test results and in conjunction with the second device data; If the instrument is fully functional, then the disinfection and drying of the target orthopedic medical instrument is deemed to be qualified. Conversely, warnings are issued based on the type of the target orthopedic medical device.

[0013] Preferably, the comparison unit includes: If there are first test sub-data in the first test data that do not fall within the scope of standard disinfection and drying data, then the first test sub-data that does not fall within the scope of standard disinfection and drying data is extracted and the data is integrated to obtain the second test data; Obtain the data type of each test sub-data in the second test data, and extract the second instrument data related to each data type to obtain the third instrument data; At the same time, it is necessary to determine whether the second test data belongs to a defect in the disinfection process or a defect in the drying process; If the second test data indicates a defect in the disinfection process, the target medical orthopedic device number related to the third device data is obtained, and the corresponding target medical orthopedic device is disinfected. If the second inspection data is a defect in the drying process, the target medical orthopedic device number related to the third device data is obtained, and the corresponding target medical orthopedic device is dried. If the second inspection data contains defects in the disinfection process and the drying process, the target medical orthopedic device number related to the third device data is obtained, and the corresponding target medical orthopedic device is disinfected and dried.

[0014] This invention provides an automated sterilization and drying method for medical orthopedic instruments, used to execute any one of the automated sterilization and drying devices for medical orthopedic instruments in Examples 1 to 8, comprising: S1: Based on preset sensors, make a preliminary judgment on the target orthopedic medical device and obtain real-time device data of the target orthopedic medical device. S2: Combine the instrument material and the disinfection requirements of the target orthopedic medical instrument with real-time instrument data to determine the intelligent disinfection plan for the target orthopedic medical instrument, and perform intelligent disinfection of the target orthopedic medical instrument based on the intelligent disinfection plan to obtain the first instrument data after disinfection. S3: Based on the first instrument data, select the drying mode with the highest matching degree to dry the target medical orthopedic instrument, thereby obtaining the second instrument data after drying; S4: Perform data verification on the second instrument data, and determine whether the target medical orthopedic instrument can meet the real-time use requirements based on the data verification results. If it does, then the disinfection and drying of the target medical orthopedic instrument is deemed qualified.

[0015] The beneficial effects of this invention compared to the prior art are as follows: by making a preliminary judgment on the target orthopedic medical device, real-time device data is obtained, and a smart disinfection scheme suitable for the target orthopedic medical device is determined in combination with the device material, disinfection requirements, etc., so as to carry out smart disinfection. After disinfection, a drying mode that can dry the target orthopedic medical device without damage is selected for drying, and the dried target orthopedic medical device is inspected, thereby improving the efficiency and accuracy of disinfection and drying, while ensuring the safe use of the device to the greatest extent.

[0016] Other features and advantages of the invention will be set forth in the description which follows, and will be apparent in part from the description, or may be learned by practicing the invention. The objects and other advantages of the invention may be realized and obtained by means of the structures particularly pointed out in this application.

[0017] The technical solution of the present invention will be further described in detail below with reference to the accompanying drawings and embodiments. Attached Figure Description

[0018] The accompanying drawings are provided to further illustrate the invention and form part of the specification. They are used in conjunction with embodiments of the invention to explain the invention and do not constitute a limitation thereof. In the drawings: Figure 1 This is a structural diagram of an automatic disinfection and drying device for medical orthopedic instruments according to an embodiment of the present invention; Figure 2 This is a schematic diagram of an automatic disinfection and drying method for medical orthopedic instruments according to an embodiment of the present invention. Detailed Implementation

[0019] The preferred embodiments of the present invention will be described below with reference to the accompanying drawings. It should be understood that the preferred embodiments described herein are for illustration and explanation only and are not intended to limit the present invention.

[0020] Example 1: This invention provides an automatic sterilization and drying device for medical orthopedic instruments, comprising: The instrument processing module is used to make a preliminary judgment on the target orthopedic medical instrument based on preset sensors, and to obtain real-time instrument data of the target orthopedic medical instrument in the preliminary judgment. The intelligent disinfection module is used to determine an intelligent disinfection plan for the target orthopedic medical device by combining the device material and the disinfection requirements of the target orthopedic medical device with real-time device data, and to perform intelligent disinfection of the target orthopedic medical device based on the intelligent disinfection plan, thereby obtaining the first device data after disinfection. The drying module is used to dry the target orthopedic medical device by selecting the drying mode with the highest matching degree based on the first device data, thereby obtaining the second device data after drying. The equipment inspection module is used to inspect the data of the second instrument, and then determine whether the target medical orthopedic instrument can meet the real-time use requirements based on the data inspection results. If it does, the disinfection and drying of the target medical orthopedic instrument is deemed qualified.

[0021] In this embodiment, preset sensors are pre-installed in the system to monitor and collect relevant data from the target orthopedic medical device. For example, preset sensors include temperature sensors, humidity sensors, and light sensors, depending on the parameters to be monitored.

[0022] In this embodiment, the preliminary judgment is based on data from preset sensors. The system makes a preliminary assessment of the status of the target orthopedic medical device, such as determining whether the device is clean or damaged.

[0023] In this embodiment, real-time device data is various data about the target medical orthopedic device, such as temperature, humidity, and location, collected in real time by preset sensors.

[0024] In this embodiment, the instrument material refers to the material used in the target orthopedic medical instrument, such as stainless steel or titanium alloy. Different materials have different tolerances to disinfection methods and disinfectants.

[0025] In this embodiment, the disinfection requirement depends on the usage scenario of the target orthopedic medical device and the patient's health condition. For example, the disinfection requirement may be higher for high-risk surgeries.

[0026] In this embodiment, the intelligent disinfection plan is automatically generated by the system based on the instrument material, disinfection requirements, and real-time instrument data. This plan may include parameters such as the type and concentration of the disinfectant, and the disinfection time.

[0027] In this embodiment, the first instrument data is the data about the target medical orthopedic instrument collected by the system again through sensors after the intelligent disinfection is completed, which is used to evaluate the disinfection effect.

[0028] In this embodiment, the drying mode is one of a variety of preset drying programs, each of which has specific drying methods, drying temperatures, time, humidity and other parameters.

[0029] In this embodiment, the drying mode with the highest matching degree is to select the most suitable drying program for the current instrument from the preset drying modes based on the first instrument data after disinfection (such as material, humidity, etc.).

[0030] In this embodiment, the second device data is the data about the target medical orthopedic device collected again by the system through sensors after drying is completed, which is used to evaluate the drying effect.

[0031] In this embodiment, data verification involves a series of checks and analyses of the data of the dried second instrument to ensure that the condition of the instrument meets the usage standards.

[0032] In this embodiment, the real-time usage requirements depend on the specific requirements of the surgery or treatment in which the target orthopedic medical device will be used. For example, for aseptic surgery, the device must meet certain aseptic standards.

[0033] In this embodiment, "disinfection and drying qualified" means that the data of the second instrument has passed the data verification and meets the requirements for real-time use. Therefore, it is determined that the disinfection and drying process of the target medical orthopedic instrument is qualified and can be used safely.

[0034] The beneficial effects of the above technology are as follows: by making a preliminary judgment on the target orthopedic medical device, real-time device data is obtained, and a smart disinfection plan that meets the requirements of the target orthopedic medical device is determined in combination with the device material and disinfection requirements, so as to carry out smart disinfection. After disinfection, a drying mode that can dry the target orthopedic medical device without damage is selected for drying, and the dried target orthopedic medical device is inspected, thereby improving the efficiency and accuracy of disinfection and drying, while ensuring the safe use of the device to the greatest extent.

[0035] Example 2: Based on Example 1, an automatic sterilization and drying device for medical orthopedic instruments, including an instrument processing module, comprises: Preliminary identification unit: used to perform preliminary identification of target orthopedic medical devices based on preset sensors to obtain initial device data; Type determination unit: used to classify the target orthopedic medical device by type based on the initial device data, and obtain the first set of device types of the target orthopedic medical device; Comprehensive Judgment Unit: Used to combine the first set of instrument types with the initial instrument data to determine whether the target medical orthopedic instrument needs to be disinfected and dried; If the target orthopedic medical device needs to be sterilized and dried, the initial device data will be standardized to obtain the real-time device data of the target orthopedic medical device. Conversely, there is no need to sterilize and dry the target orthopedic medical device.

[0036] In this embodiment, the preset sensor is pre-set to detect specific attributes or states of the target orthopedic medical device. Examples include temperature sensors, humidity sensors, and weight sensors, depending on the type of data to be detected.

[0037] In this embodiment, preliminary identification refers to using preset sensors to perform preliminary perception and identification of the target orthopedic medical device in order to obtain its basic information or status.

[0038] In this embodiment, the initial device data is a set of data obtained after the target orthopedic medical device has been initially identified by preset sensors. For example, the initial device data includes basic information such as the device's temperature, humidity, weight, and size.

[0039] In this embodiment, device type classification refers to categorizing target orthopedic medical devices into specific types or categories based on the characteristics of initial device data. The purpose of classification is to enable more accurate processing and analysis of different types of devices.

[0040] In this embodiment, the first device type set is the result obtained after device type classification, that is, the set of specific types or categories to which the target medical orthopedic device is classified.

[0041] In this embodiment, data standardization refers to transforming or adjusting the initial instrument data to conform to certain standards or formats. The aim is to improve the accuracy and comparability of the data, providing a reliable basis for subsequent processing.

[0042] In this embodiment, the real-time device data is a set of data of the target medical orthopedic device obtained after data standardization processing. Compared with the initial device data, the real-time device data is more accurate and reliable, and conforms to certain standards or formats.

[0043] In this embodiment, disinfection and drying refers to the process of cleaning, disinfecting, and drying the target orthopedic medical device. Disinfection is to kill or remove microorganisms on the device to ensure its sterility; drying is to remove moisture from the device to prevent the growth of bacteria or mold.

[0044] The beneficial effects of the above technologies are as follows: by identifying and determining the type of the target orthopedic medical device and combining it with the initial device data to determine the real-time device data, the determination of the intelligent disinfection plan for the target orthopedic medical device becomes more accurate, thereby improving the accuracy of disinfection and drying.

[0045] Example 3: Based on Example 2, an automatic sterilization and drying device for medical orthopedic instruments, including an intelligent sterilization module, comprises: Solution screening unit: used to identify the material of the target medical orthopedic device based on preset sensors, and determine the disinfection treatment plan for each target medical orthopedic device based on the preset material database, so as to obtain an initial disinfection treatment plan table; Disinfection treatment unit: used to extract the disinfection treatment plan that meets the requirements of each target medical orthopedic device based on the initial disinfection treatment plan table, and use it as the initial disinfection treatment plan; Disinfection optimization unit: used to determine the number of target orthopedic medical instruments based on real-time instrument data, and optimize the initial disinfection treatment plan based on the number of instruments to obtain an optimized disinfection plan; The second optimization unit is used to obtain the real-time usage requirements of the target medical orthopedic device to determine the corresponding disinfection requirements, and to optimize the disinfection optimization scheme based on the disinfection requirements to obtain the second optimization scheme. Disinfection scheme unit: used to input the second optimized scheme and real-time instrument data into the preset disinfection treatment model, thereby determining the intelligent disinfection scheme for the target medical orthopedic instrument; Parameter adjustment unit: used to acquire the real-time equipment parameters of the target disinfection and drying equipment, and to determine the parameter adjustment strategy for the target disinfection and drying equipment based on the intelligent disinfection scheme and the real-time equipment parameters. Strategy execution unit: used to adjust the strategy based on parameters and transmit it to the target disinfection and drying equipment for intelligent disinfection; Status detection unit: used to acquire the equipment status parameters at each detection moment of the current intelligent disinfection cycle when intelligently disinfecting the target disinfection and drying equipment, and obtain the equipment status parameter set; Parameter classification unit: used to classify the set of device status parameters based on different device types to obtain the first category parameter set; Performance Analysis Unit: Used to sort the equipment status parameters of each subset of the first category parameter set based on time series, thereby comprehensively judging the equipment stability performance of the target disinfection and drying equipment based on the sorting results, and optimizing the intelligent disinfection scheme in a timely manner based on the equipment stability performance; Data extraction unit: Used to collect real-time instrument data of the target medical orthopedic instrument after intelligent disinfection, and to process the data to obtain the first instrument data.

[0046] In this embodiment, material identification is the process of detecting and identifying the material of the target medical orthopedic device using a preset sensor.

[0047] In this embodiment, the preset material database is a database containing various medical orthopedic device materials and their corresponding disinfection treatment schemes. The system determines the disinfection treatment scheme for each device by matching the preset material database.

[0048] In this embodiment, the disinfection treatment plan is a detailed plan for disinfection steps, types of disinfectants, disinfection time, etc., formulated for medical orthopedic devices of specific materials and types.

[0049] In this embodiment, the initial disinfection treatment protocol table is a table that summarizes the preliminary disinfection treatment protocols for all target orthopedic medical devices.

[0050] In this embodiment, real-time device data refers to various data about the target orthopedic medical device, such as temperature, humidity, and location, collected in real time by sensors.

[0051] In this embodiment, the number of instruments refers to the total number of the target orthopedic medical instruments. The number of instruments is an important factor to consider when optimizing the sterilization process.

[0052] In this embodiment, the scheme optimization is the process of adjusting and improving the initial disinfection treatment scheme based on real-time instrument data and the number of instruments.

[0053] In this embodiment, the disinfection requirements are determined based on the real-time usage needs of the target orthopedic medical device, defining the disinfection standards and requirements. These requirements determine the rigor and method of disinfection procedures.

[0054] In this embodiment, the second optimization scheme is the result of further optimization of the disinfection treatment scheme after taking into account the disinfection requirements and the number of instruments.

[0055] In this embodiment, the preset disinfection treatment model is a model built based on machine learning or artificial intelligence algorithms, which is used to determine the best intelligent disinfection solution based on input data (such as the second optimization scheme and real-time instrument data).

[0056] In this embodiment, the target disinfection and drying equipment is a device used to perform intelligent disinfection and drying tasks. These devices may include various disinfection cabinets, dryers, etc.

[0057] In this embodiment, the real-time equipment parameters are various parameters collected in real time during the operation of the target disinfection and drying equipment, such as temperature, humidity, and pressure, which are used to adjust the working status of the equipment.

[0058] In this embodiment, the parameter adjustment strategy is a device parameter adjustment plan based on the intelligent disinfection scheme and real-time device parameters. The parameter adjustment strategy ensures that the device can operate according to the predetermined disinfection scheme.

[0059] In this embodiment, intelligent disinfection is an automated and intelligent disinfection process that utilizes a preset disinfection treatment model and parameter adjustment strategy to disinfect the target medical orthopedic device.

[0060] In this embodiment, the detection time is the time point at which the system periodically collects the device status parameters during the intelligent disinfection cycle.

[0061] In this embodiment, the device status parameter set is the set of all device status parameters collected by the system during the intelligent disinfection cycle.

[0062] In this embodiment, the first classification parameter set is a parameter set obtained by classifying the device status parameter set according to the device type.

[0063] In this embodiment, equipment stability performance refers to the ability of the target disinfection and drying equipment to maintain stable operation during the intelligent disinfection process, which is an important indicator for evaluating equipment performance.

[0064] In this embodiment, the first instrument data is the data of the target medical orthopedic instrument that the system collects and processes in real time after intelligent disinfection is completed, and is used to evaluate the disinfection effect and instrument status.

[0065] The beneficial effects of the above technologies are as follows: by combining the material of the instrument and the disinfection requirements to determine an intelligent disinfection plan that meets the target medical orthopedic instruments, intelligent disinfection can be carried out, and the stability performance of the equipment can be monitored in real time to optimize the intelligent disinfection plan in a timely manner. This can improve the efficiency and accuracy of disinfection, thereby ensuring the safe use of the instruments to the greatest extent.

[0066] Example 4: Based on Example 3, an automatic sterilization and drying device for medical orthopedic instruments, including a performance analysis unit, comprises: First sorting subunit: used to sort the device status parameters of each first category parameter subset in the first category parameter set based on the time series, to obtain the first ordered parameter set; Curve fitting subunit: Used to input the device state parameters in each first ordered parameter subset of the first ordered parameter set into the same coordinate system and perform curve fitting to obtain the first state parameter curve corresponding to each first ordered parameter subset; Performance Judgment Subunit: Used to judge the parameter performance of the equipment state parameter corresponding to each first state parameter curve based on the degree of curve fluctuation of the first state parameter curve, so as to comprehensively determine the equipment stability performance of the target disinfection and drying equipment.

[0067] In this embodiment, the time series refers to the device status parameters recorded at the detection time within the intelligent disinfection cycle.

[0068] In this embodiment, the first classification parameter set is a parameter set obtained by classifying the device status parameter set according to the device type (such as disinfection cabinet, dryer, etc.). Each first classification parameter set contains all status parameters of the same type of device.

[0069] In this embodiment, the first classification parameter subset is a set of state parameters for a single device or multiple detection times of the same device within the first classification parameter set. It is a subset of the first classification parameter set.

[0070] In this embodiment, the first ordered parameter set is obtained by sorting the device status parameters in the first categorized parameter subset based on time series. This ensures that the parameters are arranged in chronological order, facilitating analysis.

[0071] In this embodiment, the first ordered parameter subset is an ordered set of state parameters for a single device within the first ordered parameter set.

[0072] In this embodiment, curve fitting is the process of connecting the device state parameters into a smooth curve using mathematical methods (such as polynomial fitting, exponential fitting, etc.).

[0073] In this embodiment, the first state parameter curve is obtained through curve fitting and describes the change of device state parameters over time. Each first state parameter curve corresponds to a first ordered subset of parameters.

[0074] In this embodiment, the degree of curve fluctuation describes the drastic change of the curve over time.

[0075] In this embodiment, parameter performance refers to the behavior or characteristics of equipment state parameters under specific conditions. Parameter performance is comprehensively evaluated through curve fluctuation, stability index, and outlier index.

[0076] In this embodiment, equipment stability performance refers to the ability of the target disinfection and drying equipment to maintain stable operation during the intelligent disinfection process. Equipment stability performance is determined by comprehensively evaluating the performance of multiple equipment status parameters.

[0077] The beneficial effects of the above technologies are as follows: by real-time detection and analysis of equipment stability performance, intelligent disinfection solutions can be optimized in a timely manner, thereby improving the efficiency and accuracy of disinfection and ensuring the safe use of instruments to the greatest extent.

[0078] Example 5: Based on Example 4, an automatic sterilization and drying device for medical orthopedic instruments includes a performance judgment subunit, comprising: The parameter performance Z of the device state parameter corresponding to each first state parameter curve is determined based on the degree of curve fluctuation of the first state parameter curve. Where Z represents the parametric performance of the current first state parameter curve. The exponential weight of the stability index of the current first state parameter curve. The exponential weight of the fluctuation exponent of the current first state parameter curve. The exponential weight of the outlier index of the current first state parameter curve is given by N, where N is the number of state parameter points in the current first state parameter curve. This represents the difference between the parameter value corresponding to the state parameter point in the current first state parameter curve and the corresponding value on the first state parameter curve. This represents the state parameter value corresponding to the i-th state parameter point in the current first state parameter curve. Let be the curve parameter value corresponding to the i-th state parameter point in the current first state parameter curve, and b be the maximum parameter difference corresponding to the current first state parameter curve. Let be the standard deviation of the curve parameter value corresponding to each state parameter point in the first state parameter curve, m be the average value of the curve parameter value corresponding to each state parameter point in the first state parameter curve, and e be the logarithm of the natural base. The value is less than 10.

[0079] Conversely, there is no need to sterilize and dry the target orthopedic medical device.

[0080] In this embodiment, the curve parameter value refers to the parameter value corresponding to each state parameter point after curve fitting.

[0081] In this embodiment, the state parameter value refers to the initial parameter value corresponding to each state parameter point. The state parameter value is the parameter value that has not been curve fitted. The state parameter value can be the same as the curve parameter value or different from the curve parameter value.

[0082] The beneficial effects of the above technologies are as follows: by calculating the performance parameters of the equipment status parameters, the stability performance of the equipment can be comprehensively judged, and the intelligent disinfection scheme can be optimized in a timely manner, which can improve the efficiency and accuracy of disinfection, thereby ensuring the safe use of instruments to the greatest extent.

[0083] Example 6: Based on Example 3, an automatic sterilization and drying device for medical orthopedic instruments, including a drying module, comprises: Drying comparison unit: used to compare the first instrument data with each drying mode in the drying database, thereby extracting the drying mode with the highest matching degree with the first instrument data as the first drying mode; Drying strategy unit: used to determine the equipment parameter adjustment strategy for the target disinfection and drying equipment based on the first drying mode; Drying execution unit: used to dry the target medical orthopedic device based on the equipment parameter adjustment strategy, and to obtain the real-time device data after drying based on the preset sensors to obtain the second device data of the target medical orthopedic device.

[0084] In this embodiment, the drying database is a database that stores various drying modes and their related parameters. Each drying mode is optimized for a specific instrument type, material, or post-sterilization state to ensure the best drying effect.

[0085] In this embodiment, the drying mode is a preset scheme in the drying database, which defines key parameters such as temperature, humidity, and time during the drying process. Different drying modes are suitable for different types of medical devices or different drying needs.

[0086] In this embodiment, the matching degree refers to the similarity or applicability between the first instrument data and various drying modes in the drying database. The system determines which drying mode is most suitable for the current instrument state by comparing the first instrument data with the preset parameters of each drying mode.

[0087] In this embodiment, the first drying mode is the drying mode with the highest matching degree with the first instrument data. The system selects the most suitable drying scheme for the current instrument condition from the drying database through comparison and evaluation.

[0088] In this embodiment, the equipment parameter adjustment strategy is a parameter adjustment plan for the target disinfection and drying equipment formulated by the system based on the first drying mode. The equipment parameter adjustment strategy describes how to adjust parameters such as temperature, humidity, and time of the drying equipment to ensure that the drying process is carried out in accordance with the first drying mode.

[0089] In this embodiment, instrument drying refers to the process of drying the target orthopedic medical instrument. During the drying process, the system adjusts the operation of the drying equipment according to the equipment parameters to ensure that the instrument achieves the expected drying effect.

[0090] In this embodiment, the second instrument data is real-time instrument data acquired by the system through preset sensors after the instrument has been dried. This includes key indicators such as temperature, humidity, and surface dryness after drying, used to evaluate the drying effect and confirm whether the instrument has met the standards for safe use.

[0091] The beneficial effects of the above technology are as follows: by combining the first instrument data to extract the drying mode with the highest matching degree as the first drying mode of the target disinfection and drying equipment, and adjusting the equipment parameters to the first drying mode state, the drying of the target medical orthopedic instruments can better meet the real-time drying needs and improve the drying efficiency.

[0092] Example 7: Based on Example 6, an automatic sterilization and drying device for medical orthopedic instruments, including a testing module, comprises: Data verification unit: used to verify the second device data based on the disinfection and drying requirements of the target medical orthopedic device, thereby obtaining the first verification data; The comparison unit is used to compare the first test data with the standard disinfection and drying data range. If each initial test data falls within the standard sterilization and drying data range, the initial test of the target medical orthopedic device is deemed qualified. If any of the first test data is not within the range of standard disinfection and drying data, the target medical orthopedic device needs to be disinfected and dried again. Functional testing unit: used to determine the functional integrity of the target orthopedic medical device based on the initial qualified test results and in conjunction with the second device data; If the instrument is fully functional, then the disinfection and drying of the target orthopedic medical instrument is deemed to be qualified. Conversely, warnings are issued based on the type of the target orthopedic medical device.

[0093] In this embodiment, data verification refers to the process of validating and confirming the data of the second instrument to ensure that the data meets the expected sterilization and drying standards. This typically involves comparison and analysis with preset standard data.

[0094] In this embodiment, the first test data is key data related to the standard disinfection and drying requirements, obtained after data verification, and is used to evaluate whether the instrument has achieved the expected disinfection and drying effect.

[0095] In this embodiment, the standard sterilization and drying data range is a preset data range used to define the standards that the instrument data should meet after sterilization and drying. The data range is based on experimental data, industry standards, or manufacturer recommendations.

[0096] In this embodiment, initial inspection qualification means that after data inspection, it is confirmed that each first inspection data is within the range of standard disinfection and drying data, thereby judging that the disinfection and drying treatment of the target medical orthopedic device has reached the preliminary qualification standard.

[0097] In this embodiment, the first test sub-data is a subset or component of the first test data, used to evaluate the disinfection and drying effect in a specific aspect. If a certain first test sub-data does not meet the standard, it means that the treatment in that aspect has not achieved the expected effect.

[0098] In this embodiment, the disinfection and drying process refers to the additional disinfection and drying process required for the target medical orthopedic device if there are non-compliant data in the first inspection data, in order to ensure that it achieves the expected disinfection and drying effect.

[0099] In this embodiment, device functional integrity refers to whether the target orthopedic medical device retains all its functions intact and normal after sterilization and drying. This typically involves an assessment of the device's mechanical properties, electrical properties, and safety of use.

[0100] In this embodiment, "disinfection and drying qualified" means that the target medical orthopedic device has met the expected standards and requirements after disinfection and drying treatment and functional integrity assessment, and is therefore judged to be qualified.

[0101] The beneficial effects of the above technology are as follows: by inspecting the instruments after disinfection and drying, the disinfection and drying results can be judged, and timely warnings can be issued for unqualified instruments, which can ensure the safe use of instruments to the greatest extent.

[0102] Example 8: Based on Example 7, an automatic sterilization and drying device for medical orthopedic instruments, including a testing and comparison unit, comprises: If there are first test sub-data in the first test data that do not fall within the scope of standard disinfection and drying data, then the first test sub-data that does not fall within the scope of standard disinfection and drying data is extracted and the data is integrated to obtain the second test data; Obtain the data type of each test sub-data in the second test data, and extract the second instrument data related to each data type to obtain the third instrument data; At the same time, it is necessary to determine whether the second test data belongs to a defect in the disinfection process or a defect in the drying process; If the second test data indicates a defect in the disinfection process, the target medical orthopedic device number related to the third device data is obtained, and the corresponding target medical orthopedic device is disinfected. If the second inspection data is a defect in the drying process, the target medical orthopedic device number related to the third device data is obtained, and the corresponding target medical orthopedic device is dried. If the second inspection data contains defects in the disinfection process and the drying process, the target medical orthopedic device number related to the third device data is obtained, and the corresponding target medical orthopedic device is disinfected and dried.

[0103] In this embodiment, the first test sub-data is a specific subset or data point within the first test data, used to evaluate a specific aspect or parameter in the disinfection and drying process. If the first test sub-data does not fall within the standard disinfection and drying data range, it indicates that there may be a problem with the processing of that aspect or parameter.

[0104] In this embodiment, the standard disinfection and drying data range is a preset range used to define the standard that the instrument data should meet after disinfection and drying. If the test data exceeds this range, it indicates that the treatment effect may not meet the standard.

[0105] In this embodiment, the second test data is a set of data obtained by extracting the first test sub-data that does not fall within the scope of standard disinfection and drying data and then synthesizing the data.

[0106] In this embodiment, the data type refers to the category or classification of data, such as temperature, humidity, pressure, time, etc. Obtaining the data type of each sub-data item in the second test data is to enable the targeted extraction of second instrument data related to these data types.

[0107] In this embodiment, the third instrument data is a set of data related to each test sub-data in the second test data, extracted from the second instrument data.

[0108] In this embodiment, defects in the disinfection process refer to problems or deficiencies that occur during the disinfection process, resulting in substandard disinfection effects. For example, these defects may be caused by improper disinfection parameter settings, insufficient disinfection time, or improper use of disinfectant.

[0109] In this embodiment, the drying process defect refers to problems or deficiencies that occur during the drying process, resulting in substandard drying effects. For example, it may be caused by improper settings of parameters such as drying temperature, humidity, and time, or by malfunctions in the drying equipment.

[0110] In this embodiment, the target orthopedic medical device number is a number or code used to uniquely identify the target orthopedic medical device. When a defect is found in the sterilization or drying process, the problematic device can be accurately located by obtaining the device number associated with the third-party device data, so that subsequent processing can be carried out.

[0111] The beneficial effects of the above technology are as follows: by inspecting the instruments after disinfection and drying, the disinfection and drying results can be judged, and timely warnings and warning types can be determined for unqualified instruments. This makes the warnings for target medical orthopedic instruments more accurate, thereby improving the efficiency of instrument use and ensuring the safe use of instruments to the greatest extent.

[0112] Example 9: This invention provides an automatic sterilization and drying method for medical orthopedic instruments, used to execute any one of the automatic sterilization and drying devices for medical orthopedic instruments in Examples 1 to 8, as described above. Figure 2 ,include: S1: Based on preset sensors, make a preliminary judgment on the target orthopedic medical device and obtain real-time device data of the target orthopedic medical device. S2: Combine the instrument material and the disinfection requirements of the target orthopedic medical instrument with real-time instrument data to determine the intelligent disinfection plan for the target orthopedic medical instrument, and perform intelligent disinfection of the target orthopedic medical instrument based on the intelligent disinfection plan to obtain the first instrument data after disinfection. S3: Based on the first instrument data, select the drying mode with the highest matching degree to dry the target medical orthopedic instrument, thereby obtaining the second instrument data after drying; S4: Perform data verification on the second instrument data, and determine whether the target medical orthopedic instrument can meet the real-time use requirements based on the data verification results. If it does, then the disinfection and drying of the target medical orthopedic instrument is deemed qualified.

[0113] The beneficial effects of the above technology are as follows: by making a preliminary judgment on the target orthopedic medical device, real-time device data is obtained, and a smart disinfection plan that meets the requirements of the target orthopedic medical device is determined in combination with the device material and disinfection requirements, so as to carry out smart disinfection. After disinfection, a drying mode that can dry the target orthopedic medical device without damage is selected for drying, and the dried target orthopedic medical device is inspected, thereby improving the efficiency and accuracy of disinfection and drying, while ensuring the safe use of the device to the greatest extent.

[0114] Obviously, those skilled in the art can make various modifications and variations to this invention without departing from its spirit and scope. Therefore, if these modifications and variations fall within the scope of the claims of this invention and their equivalents, this invention also intends to include these modifications and variations.

Claims

1. An automatic sterilization and drying device for medical orthopedic instruments, characterized in that, include: The instrument processing module is used to make a preliminary judgment on the target orthopedic medical instrument based on preset sensors, and to obtain real-time instrument data of the target orthopedic medical instrument in the preliminary judgment. The intelligent disinfection module is used to determine an intelligent disinfection plan for the target orthopedic medical device by combining the device material and the disinfection requirements of the target orthopedic medical device with real-time device data, and to perform intelligent disinfection of the target orthopedic medical device based on the intelligent disinfection plan, thereby obtaining the first device data after disinfection. The drying module is used to dry the target orthopedic medical device by selecting the drying mode with the highest matching degree based on the first device data, thereby obtaining the second device data after drying. The equipment inspection module is used to inspect the data of the second instrument, and then determine whether the target medical orthopedic instrument can meet the real-time use requirements based on the data inspection results. If it does, the disinfection and drying of the target medical orthopedic instrument is deemed qualified.

2. The automatic disinfection and drying equipment for medical orthopedic instruments according to claim 1, characterized in that, The instrument processing module includes: Preliminary identification unit: used to perform preliminary identification of target orthopedic medical devices based on preset sensors to obtain initial device data; Type determination unit: used to classify the target orthopedic medical device by type based on the initial device data, and obtain the first set of device types of the target orthopedic medical device; Comprehensive Judgment Unit: Used to combine the first set of instrument types with the initial instrument data to determine whether the target medical orthopedic instrument needs to be disinfected and dried; If the target orthopedic medical device needs to be sterilized and dried, the initial device data will be standardized to obtain the real-time device data of the target orthopedic medical device. Conversely, there is no need to sterilize and dry the target orthopedic medical device.

3. The automatic sterilization and drying equipment for medical orthopedic instruments according to claim 2, characterized in that, The intelligent disinfection module includes: Solution screening unit: used to identify the material of the target medical orthopedic device based on preset sensors, and determine the disinfection treatment plan for each target medical orthopedic device based on the preset material database, so as to obtain an initial disinfection treatment plan table; Disinfection treatment unit: used to extract the disinfection treatment plan that meets the requirements of each target medical orthopedic device based on the initial disinfection treatment plan table, and use it as the initial disinfection treatment plan; Disinfection optimization unit: used to determine the number of target orthopedic medical instruments based on real-time instrument data, and optimize the initial disinfection treatment plan based on the number of instruments to obtain an optimized disinfection plan; The second optimization unit is used to obtain the real-time usage requirements of the target medical orthopedic device to determine the corresponding disinfection requirements, and to optimize the disinfection optimization scheme based on the disinfection requirements to obtain the second optimization scheme. Disinfection scheme unit: used to input the second optimized scheme and real-time instrument data into the preset disinfection treatment model, thereby determining the intelligent disinfection scheme for the target medical orthopedic instrument; Parameter adjustment unit: used to acquire the real-time equipment parameters of the target disinfection and drying equipment, and to determine the parameter adjustment strategy for the target disinfection and drying equipment based on the intelligent disinfection scheme and the real-time equipment parameters. Strategy execution unit: used to adjust the strategy based on parameters and transmit it to the target disinfection and drying equipment for intelligent disinfection; Status detection unit: used to acquire the equipment status parameters at each detection moment of the current intelligent disinfection cycle when intelligently disinfecting the target disinfection and drying equipment, and obtain the equipment status parameter set; Parameter classification unit: used to classify the set of device status parameters based on different device types to obtain the first category parameter set; Performance Analysis Unit: Used to sort the equipment status parameters of each subset of the first category parameter set based on time series, thereby comprehensively judging the equipment stability performance of the target disinfection and drying equipment based on the sorting results, and optimizing the intelligent disinfection scheme in a timely manner based on the equipment stability performance; Data extraction unit: Used to collect real-time instrument data of the target medical orthopedic instrument after intelligent disinfection, and to process the data to obtain the first instrument data.

4. The automatic disinfection and drying equipment for medical orthopedic instruments according to claim 3, characterized in that, The performance analysis unit includes: First sorting subunit: used to sort the device status parameters of each first category parameter subset in the first category parameter set based on the time series, to obtain the first ordered parameter set; Curve fitting subunit: Used to input the device state parameters in each first ordered parameter subset of the first ordered parameter set into the same coordinate system and perform curve fitting to obtain the first state parameter curve corresponding to each first ordered parameter subset; Performance Judgment Subunit: Used to judge the parameter performance of the equipment state parameter corresponding to each first state parameter curve based on the degree of curve fluctuation of the first state parameter curve, so as to comprehensively determine the equipment stability performance of the target disinfection and drying equipment.

5. The automatic disinfection and drying equipment for medical orthopedic instruments according to claim 4, characterized in that, The performance evaluation subunit includes: The parameter performance Z of the device state parameter corresponding to each first state parameter curve is determined based on the degree of curve fluctuation of the first state parameter curve. Where Z represents the parametric performance of the current first state parameter curve. The exponential weight of the stability index of the current first state parameter curve. The exponential weight of the fluctuation exponent of the current first state parameter curve. The exponential weight of the outlier index of the current first state parameter curve is given by N, where N is the number of state parameter points in the current first state parameter curve. This represents the difference between the parameter value corresponding to the state parameter point in the current first state parameter curve and the corresponding value on the first state parameter curve. This represents the state parameter value corresponding to the i-th state parameter point in the current first state parameter curve. Let be the curve parameter value corresponding to the i-th state parameter point in the current first state parameter curve, and b be the maximum parameter difference corresponding to the current first state parameter curve. Let be the standard deviation of the curve parameter value corresponding to each state parameter point in the first state parameter curve, m be the average value of the curve parameter value corresponding to each state parameter point in the first state parameter curve, and e be the logarithm of the natural base.

6. The automatic sterilization and drying equipment for medical orthopedic instruments according to claim 3, characterized in that, The drying module includes: Drying comparison unit: used to compare the first instrument data with each drying mode in the drying database, thereby extracting the drying mode with the highest matching degree with the first instrument data as the first drying mode; Drying strategy unit: used to determine the equipment parameter adjustment strategy for the target disinfection and drying equipment based on the first drying mode; Drying execution unit: used to dry the target medical orthopedic device based on the equipment parameter adjustment strategy, and to obtain the real-time device data after drying based on the preset sensors to obtain the second device data of the target medical orthopedic device.

7. The automatic sterilization and drying equipment for medical orthopedic instruments according to claim 6, characterized in that, The equipment inspection module includes: Data verification unit: used to verify the second device data based on the disinfection and drying requirements of the target medical orthopedic device, thereby obtaining the first verification data; The comparison unit is used to compare the first test data with the standard disinfection and drying data range. If each initial test data falls within the standard sterilization and drying data range, then the initial test of the target medical orthopedic device is deemed qualified. If any of the first test data is not within the range of standard disinfection and drying data, the target medical orthopedic device needs to be disinfected and dried again. Functional testing unit: used to determine the functional integrity of the target orthopedic medical device based on the initial qualified test results and in conjunction with the second device data; If the instrument is fully functional, then the disinfection and drying of the target orthopedic medical instrument is deemed to be qualified. Conversely, warnings are issued based on the type of the target orthopedic medical device.

8. The automatic sterilization and drying equipment for medical orthopedic instruments according to claim 7, characterized in that, The comparison unit includes: If there are first test sub-data in the first test data that do not fall within the scope of standard disinfection and drying data, then the first test sub-data that does not fall within the scope of standard disinfection and drying data is extracted and the data is integrated to obtain the second test data; Obtain the data type of each test sub-data in the second test data, and extract the second instrument data related to each data type to obtain the third instrument data; At the same time, it is necessary to determine whether the second test data belongs to a defect in the disinfection process or a defect in the drying process; If the second test data indicates a defect in the disinfection process, the target medical orthopedic device number related to the third device data is obtained, and the corresponding target medical orthopedic device is disinfected. If the second inspection data is a defect in the drying process, the target medical orthopedic device number related to the third device data is obtained, and the corresponding target medical orthopedic device is dried. If the second inspection data contains defects in the disinfection process and the drying process, the target medical orthopedic device number related to the third device data is obtained, and the corresponding target medical orthopedic device is disinfected and dried.

9. An automatic sterilization and drying method for medical orthopedic instruments, characterized in that, An automatic sterilization and drying device for medical orthopedic instruments according to any one of claims 1 to 8, comprising: S1: Based on preset sensors, make a preliminary judgment on the target orthopedic medical device and obtain real-time device data of the target orthopedic medical device. S2: Combine the instrument material and the disinfection requirements of the target orthopedic medical instrument with real-time instrument data to determine the intelligent disinfection plan for the target orthopedic medical instrument, and perform intelligent disinfection of the target orthopedic medical instrument based on the intelligent disinfection plan to obtain the first instrument data after disinfection. S3: Based on the first instrument data, select the drying mode with the highest matching degree to dry the target medical orthopedic instrument, thereby obtaining the second instrument data after drying; S4: Perform data verification on the second instrument data, and determine whether the target medical orthopedic instrument can meet the real-time use requirements based on the data verification results. If it does, then the disinfection and drying of the target medical orthopedic instrument is deemed qualified.

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